Canonical Allele Identifier: CA2259200850

Gene: TCAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665983G= , CM000679.2:g.39665983G=	GRCh38
NC_000017.10:g.37822236G= , CM000679.1:g.37822236G=	GRCh37
NC_000017.9:g.35075762G=	NCBI36
NG_008892.1:g.5638G= , LRG_210:g.5638G=
NG_042278.1:g.3003G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.378G= MANE Select	ENSP00000312624.2:p.Gln126=
ENST00000309889.2:c.378G=	ENSP00000312624.2:p.Gln126=
ENST00000578283.1:c.306G=	ENSP00000462787.1:p.Gln102=
NM_003673.3:c.378G= , LRG_210t1:c.378G=	NP_003664.1:p.Gln126=
NM_003673.4:c.378G= MANE Select	NP_003664.1:p.Gln126=